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Isolation of a New Caryophyllane Ester from Lactarius subumbonatus: Conformational Analysis and Absolute Configuration

✍ Scribed by Marco Clericuzio; Lucio Toma; Giovanni Vidari


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
203 KB
Volume
1999
Category
Article
ISSN
1434-193X

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✦ Synopsis


The absolute configuration of the sesquiterpene moiety has been established by theoretical Circular Dichroism sesquiterpene alcohol esterified by the unusual fatty acid (S)-(+)-6-hydroxystearic acid, has been isolated from the fruiting calculations (De Voe coupled oscillators theory) and that of the fatty acid by NMR studies of the (R)-2-methoxy-2-bodies of the Basidiomycete Lactarius subumbonatus. Both NMR data and AM1 calculations indicate that the naphthylacetic acid (2-NMA) ester. caryophyllene macrocyclic ring adopts a Ξ²Ξ² conformation.


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ChemInform Abstract: Fungal Metabolites.
✍ Marco Clericuzio; Lucio Toma; Giovanni Vidari πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 27 KB πŸ‘ 2 views

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